Product Details

SNP ID

rs4958531

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:152392277 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCTGCTGGGAGGTGAGAGTTGTGCA[C/T]GGATGACTGACATGGGAATTGGGGA

Phenotype

MIM: 605108

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NMUR2 PubMed Links

Gene Details

Gene

NMUR2

Gene Name

neuromedin U receptor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020167.4	1328	Missense Mutation	ATG,GTG	M388V	NP_064552.3
XM_011537670.2	1328	Intron			XP_011535972.1

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